4.8 Article

Ammonia decomposition by ruthenium nanoparticles loaded on inorganic electride C12A7:e(-)

Journal

CHEMICAL SCIENCE
Volume 4, Issue 8, Pages 3124-3130

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3sc50794g

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Funding

  1. Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST), Japan
  2. Grants-in-Aid for Scientific Research [23686115] Funding Source: KAKEN

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The use of ammonia as a hydrogen carrier has received much attention due to its high hydrogen content and liquid state under mild conditions, which could lead to fuel cell applications. This study demonstrates facile ammonia decomposition on ruthenium nanoparticles loaded on inorganic electride, C12A7:e(-). A high turnover frequency (similar to 12 s(-1) at 400 degrees C) and low activation energy (64 kJ mol(-1)) for recombinative N-2 desorption were obtained for Ru/C12A7:e(-). N-2-temperature programmed desorption (N-2-TPD) and kinetic analyses indicate that the high catalytic performance is due to the low work function of chemically stable C12A7:e(-), which enables electron injection to the antibonding orbital of the Ru-N bond formed transiently through the reaction by raising the Fermi level of Ru metal.

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